Frequency of Oral Care Intervention Study (FOCIS)
Primary Purpose
Respiratory Failure
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Tooth Brushing Protocol
Sponsored by
About this trial
This is an interventional basic science trial for Respiratory Failure focused on measuring oral care
Eligibility Criteria
Inclusion Criteria:
- within 36 hours of initial intubation,
- have at least one tooth, and
- they or their legally authorized representative are able to provide informed consent in English or Spanish.
Exclusion Criteria:
- anticipation by the clinical provider of imminent patient death, or
- medical contraindication to tooth brushing.
Sites / Locations
- Tampa General Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Experimental
Arm Label
Frequency of Once a Day
Frequency of Twice a Day
Frequency of Three Times a Day
Arm Description
Tooth Brushing Protocol to be provided at 8:00 am (+/- 1.5 hours)
Tooth Brushing Protocol to be provided at 8:00 am (+/- 1.5 hours) Tooth Brushing Protocol to be provided at 1:00 pm (+/- 1.5 hours)
Tooth Brushing Protocol to be provided at 8:00 am (+/- 1.5 hours) Tooth Brushing Protocol to be provided at 1:00 pm (+/- 1.5 hours) Tooth Brushing Protocol to be provided at 6:00 pm (+/- 1.5 hours)
Outcomes
Primary Outcome Measures
Dental Plaque as measured by University of Mississippi Oral Hygiene Index
University of Mississippi Oral Hygiene Index
Gingival Inflammation as measured by Gingival Crevicular Fluid Samples
Gingival Crevicular Fluid Samples
Secondary Outcome Measures
Systemic Inflammatory Response Syndrome as measured by SIRS Criteria
SIRS Criteria
Hospital Acquired Infection as measured by positive epidemiologic surveillance report for VAE (including VAP), bacteremia, sepsis
positive epidemiologic surveillance report for Ventilator Associated Event (including VAP), bacteremia, sepsis
Length of Hospital Stay
Number of days from hospital admission date to hospital discharge date
Length of Intubation
Number of days from intubation date to extubation date
Full Information
NCT ID
NCT02289131
First Posted
November 4, 2014
Last Updated
November 5, 2018
Sponsor
University of South Florida
Collaborators
National Institute of Nursing Research (NINR), Tampa General Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02289131
Brief Title
Frequency of Oral Care Intervention Study
Acronym
FOCIS
Official Title
Oral Care Intervention In Mechanically Ventilated Adults: Renewal
Study Type
Interventional
2. Study Status
Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
December 31, 2014 (Actual)
Primary Completion Date
March 20, 2018 (Actual)
Study Completion Date
March 20, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of South Florida
Collaborators
National Institute of Nursing Research (NINR), Tampa General Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Tooth brushing for patients with breathing tubes is routinely provided by the bedside nurse as part of clinical care. The purpose of this study is to determine how often tooth brushing should occur for adult patients with breathing tubes (mechanical ventilation), balanced with equivalence and safety.
Detailed Description
A total of 345 adult subjects who are intubated and require mechanical ventilation will be randomly assigned to one of the three different tooth brushing frequency groups: once a day, twice a day or three times a day, up to a maximum of seven days. Teeth will be brushed with a soft child size toothbrush will take approximately 2 minutes. Following tooth brushing, the mouth will be rinsed with alcohol-free mouthwash and oral fluids will be removed with an oral suction tip. Moisturizing gel will be gently applied. The complete intervention requires approximately 15 minutes.
Information will be collected will include clinical condition, medications, age, gender, and smoking status. Once every day, digital pictures will be taken of each tooth (takes approximately five minutes) using a small intraoral camera to be evaluated for plaque by a dental hygienist that is blinded to frequency group assignment. Once every day, gingival crevicular fluid samples (takes 30 seconds) to look for factors that predict infection.
Gingival crevicular fluid samples and digital pictures of the teeth will also be collected on day 1, day 3 and day 5 after extubation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Failure
Keywords
oral care
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
232 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Frequency of Once a Day
Arm Type
Experimental
Arm Description
Tooth Brushing Protocol to be provided at 8:00 am (+/- 1.5 hours)
Arm Title
Frequency of Twice a Day
Arm Type
Experimental
Arm Description
Tooth Brushing Protocol to be provided at 8:00 am (+/- 1.5 hours) Tooth Brushing Protocol to be provided at 1:00 pm (+/- 1.5 hours)
Arm Title
Frequency of Three Times a Day
Arm Type
Experimental
Arm Description
Tooth Brushing Protocol to be provided at 8:00 am (+/- 1.5 hours) Tooth Brushing Protocol to be provided at 1:00 pm (+/- 1.5 hours) Tooth Brushing Protocol to be provided at 6:00 pm (+/- 1.5 hours)
Intervention Type
Procedure
Intervention Name(s)
Tooth Brushing Protocol
Intervention Description
A 2-minute tooth brushing protocol, followed by a mouthwash rinse and application of moisturizer for a total of approximately 15 minutes.
Primary Outcome Measure Information:
Title
Dental Plaque as measured by University of Mississippi Oral Hygiene Index
Description
University of Mississippi Oral Hygiene Index
Time Frame
Participants will be followed for the duration of the study, an expected average of 10 days.
Title
Gingival Inflammation as measured by Gingival Crevicular Fluid Samples
Description
Gingival Crevicular Fluid Samples
Time Frame
Participants will be followed for the duration of the study, an expected average of 10 days.
Secondary Outcome Measure Information:
Title
Systemic Inflammatory Response Syndrome as measured by SIRS Criteria
Description
SIRS Criteria
Time Frame
Participants will be followed for the duration of the study, an expected average of 10 days.
Title
Hospital Acquired Infection as measured by positive epidemiologic surveillance report for VAE (including VAP), bacteremia, sepsis
Description
positive epidemiologic surveillance report for Ventilator Associated Event (including VAP), bacteremia, sepsis
Time Frame
Participants will be followed for the duration of the study, an expected average of 10 days.
Title
Length of Hospital Stay
Description
Number of days from hospital admission date to hospital discharge date
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 10 days.
Title
Length of Intubation
Description
Number of days from intubation date to extubation date
Time Frame
Participants will be followed for the duration of the study, an expected average of 10 days.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
within 36 hours of initial intubation,
have at least one tooth, and
they or their legally authorized representative are able to provide informed consent in English or Spanish.
Exclusion Criteria:
anticipation by the clinical provider of imminent patient death, or
medical contraindication to tooth brushing.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cindy L Munro, PhD
Organizational Affiliation
University of Miami
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kevin E Kip, PhD
Organizational Affiliation
University of South Florida
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tampa General Hospital
City
Tampa
State/Province
Florida
ZIP/Postal Code
33606
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Frequency of Oral Care Intervention Study
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