Sprixx-ICU: Evaluation of Body-worn Multimodal Hand Hygiene System. Impact on Health-Care Associated Infections

Sponsor
Dartmouth-Hitchcock Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT01050608
Collaborator
Harbor Medical Inc. (Industry)
2,954
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Study Details

Study Description

Brief Summary

Evaluate the efficacy of a multimodal hand hygiene system in the intensive care unit environment and evaluate any impact on health care associated infections.

Condition or Disease Intervention/Treatment Phase
  • Device: Body worn alcohol gel dispenser
  • Drug: 62% ethanol based hand cleanser
  • Behavioral: Educational component with regard to teaching CDC guidelines
  • Behavioral: Provider and group feedback

Detailed Description

Deploy and utilize a novel body worn hand hygiene system that incorporates provider and group specific feedback allowing hand hygiene to occur directly within the patient environment. We hypothesize that by improving provider hand hygiene we will reduce health-care associated infection rates.

Study Design

Study Type:
Observational
Actual Enrollment :
2954 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Real Time Deployment of Multimodal Personal Dispenser Hand Hygiene System in a Multidisciplinary Intensive Care Unit.
Study Start Date :
Dec 1, 2007
Actual Primary Completion Date :
Dec 1, 2009
Actual Study Completion Date :
Jan 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Sprixx Device Group

Treatment group utilizing multimodal hand hygiene device

Device: Body worn alcohol gel dispenser
Records hand hygiene events of provider and tabulates on the group level.

Drug: 62% ethanol based hand cleanser
CDC based guidelines with regard to utilization in the health care environment "the nest"

Behavioral: Educational component with regard to teaching CDC guidelines
12 minute education prior to deploying device for all providers.

Behavioral: Provider and group feedback
Provide feedback with regard to expected hand hygiene goals to providers and reported anonymous group results based on recorded information.

Standard Hand Hygiene Group

Utilizing wall mounted dispensers and CDC based guidelines.

Outcome Measures

Primary Outcome Measures

  1. Reduction in healthcare associated infections (CRBSI and VAP) [2 years]

Secondary Outcome Measures

  1. Time to infections Hospital mortality Length of stay [2 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • All ICU patients
Exclusion Criteria:
  • Patient is not in an ICU at our Institution

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dartmouth-HItchcock Medical Center Lebanon New Hampshire United States 03756

Sponsors and Collaborators

  • Dartmouth-Hitchcock Medical Center
  • Harbor Medical Inc.

Investigators

  • Principal Investigator: Matthew D. Koff, M.D. M.S., Dartmouth-Hitchcock Medical Center
  • Principal Investigator: Randy L Loftus, M.D., Dartmouth-Hitchcock Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT01050608
Other Study ID Numbers:
  • 20655-ICU extension
First Posted:
Jan 15, 2010
Last Update Posted:
Jun 23, 2011
Last Verified:
Jun 1, 2011

Study Results

No Results Posted as of Jun 23, 2011