- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01192841
Bacterial Contamination of Workwear
August 30, 2010 updated by: Denver Health and Hospital Authority
Physician Dress Code And Microbial Colonization Of The White Coat: Does Physician Dress Code Alter Bacterial Colonization Rate On The Clothing Of Physicians?
Governmental agencies in the United Kingdom and Scotland have recently instituted guidelines banning physicians' white coats and wearing of long-sleeved garments to decrease hospital transmission of bacteria.
The purpose of this study is to compare the bacterial contamination of physicians' white coats with that of newly laundered, standardized short-sleeved uniforms after an eight-hour workday and to determine the rate at which bacterial contamination of the uniform ensues.
Our hypothesis was that the physician white coat would have more bacterial contamination at the end of the work day.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Governmental agencies in the United Kingdom and Scotland have recently instituted guidelines banning physicians' white coats and wearing of long-sleeved garments to decrease nosocomial transmission of bacteria.
Our goal was to compare the degree of bacterial and methicillin-resistant Staphylococcus aureus contamination of physicians' white coats with that of newly laundered, standardized short-sleeved uniforms after an eight-hour workday and to determine the rate at which bacterial contamination of the uniform ensues.
100 interns, residents, and hospitalists on an internal medicine service were randomized to wear either physician white coat or newly laundered, short-sleeved uniform.
Bacterial colony counts and the frequency with which methicillin-resistant Staphylococcus aureus was found was compared in the two groups and over time.
Our initial hypothesis was that physician white coats would have more bacterial contamination at the end of the work day.
Study Type
Interventional
Enrollment (Actual)
110
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Colorado
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Denver, Colorado, United States, 80204
- Denver Health
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Internal medicine interns, residents, and hospitalists working on acute medicine ward service.
Exclusion Criteria:
- Not willing/unable to participate in study
- Not working a full 8 hour day in the hospital
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: White coat group
Participants continued their regular practice of wearing their physician white coat.
|
|
Experimental: Uniform group
Participants were given a clean uniform (scrubs) at the beginning of the day.
|
Participants were given a clean uniform (scrubs) on the day of the study.
They wore this for approximately 8 hours.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Bacterial colony counts and the frequency with which methicillin-resistant Staphylococcus aureus was found over time
Time Frame: 8 hours
|
8 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Marisha Burden, MD, Denver Health and Housing Authority
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2008
Primary Completion (Actual)
November 1, 2009
Study Completion (Actual)
November 1, 2009
Study Registration Dates
First Submitted
August 30, 2010
First Submitted That Met QC Criteria
August 30, 2010
First Posted (Estimate)
September 1, 2010
Study Record Updates
Last Update Posted (Estimate)
September 1, 2010
Last Update Submitted That Met QC Criteria
August 30, 2010
Last Verified
August 1, 2010
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 07-1137
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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