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

Real Time Deployment of Multimodal Personal Dispenser Hand Hygiene System in a Multidisciplinary Intensive Care Unit.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01050608
Acronym
Sprixx-ICU
Enrollment
2954
Registered
2010-01-15
Start date
2007-12-31
Completion date
2011-01-31
Last updated
2011-06-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nosocomial Infection

Keywords

Alcohol Rub, Hand Hygiene, Provider Feedback, Health Care Associated Infections

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.

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.

Interventions

DEVICEBody worn alcohol gel dispenser

Records hand hygiene events of provider and tabulates on the group level.

DRUG62% ethanol based hand cleanser

CDC based guidelines with regard to utilization in the health care environment the nest

BEHAVIORALEducational component with regard to teaching CDC guidelines

12 minute education prior to deploying device for all providers.

BEHAVIORALProvider and group feedback

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

Sponsors

Harbor Medical Inc.
CollaboratorINDUSTRY
Dartmouth-Hitchcock Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* All ICU patients

Exclusion criteria

* Patient is not in an ICU at our Institution

Design outcomes

Primary

MeasureTime frame
Reduction in healthcare associated infections (CRBSI and VAP)2 years

Secondary

MeasureTime frame
Time to infections Hospital mortality Length of stay2 years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026