- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05612672
Evaluation of GeoHAI Implementation
April 29, 2026 updated by: Courtney Hebert, Ohio State University
GeoHAI Implementation in IP Workflow
Geographic Information Systems (GIS) and spatial analysis have become important tools in public health informatics but have rarely been applied to the hospital setting.
In this study we apply these tools to address the challenge of Hospital Acquired Infections (HAIs) by building, implementing, and evaluating a new computer application which incorporates mapping and geographic data to assist hospital epidemiologists in identifying HAI clusters and assessing transmission risk.
We expect that incorporation of geographic information into the workflow of hospital epidemiologists will have a profound effect on our understanding of disease transmission and HAI risk factors in the hospital setting, radically altering the workflow and speed of response of infection preventionists and improving their ability to prevent HAIs.
Study Overview
Status
Active, not recruiting
Intervention / Treatment
Detailed Description
Hospital Acquired Infections are common, affecting 3.2% of acute care hospital admissions.
Recent reports have shown an improvement in overall HAI rates, primarily driven by improvements in surgical site (SSI) and catheter associated urinary tract infections (CAUTI).
Transmissible infections, such as Clostridium difficile (CDI), have not shown the same decrease over time.
This may be because prevention of CDI requires a comprehensive hospital-wide approach addressing environmental and patient-level risk factors.
Geographic Information Systems (GIS) and spatial analysis techniques have become an important tool in public health informatics because they can integrate a vast number of data sources and explore associations and patterns in the data not visible using traditional biostatistical methods.
Applications of GIS and spatial analysis are wide ranging but have largely been ignored in the hospital setting.
The objective of this research is to develop a HAI assessment tool, which incorporates geographic data on the hospital and patient-level data from the electronic health record system, that is useful for hospital infection preventionists in better identifying clusters of HAI and assessing potential risk.
We bring together a multidisciplinary team of clinical, operational, and academic investigators with expertise in GIS and spatial analysis, patient safety, public health informatics, usability assessment, and mixed- methods evaluation.
As part of a larger study, this aim will seek to implement a GeoHAI tool that uses spatio-temporal Bayesian models to identify clusters of NHSN-defined hospital onset CDI and multidrug resistant organisms (MDRO) and predict potential high risk areas given hospital and patient risk factors.
Unique to our approach is an evaluation strategy that focuses on the reduction of hospital acquired infection, but also seeks to understand how the tool and the information derived from the tool impacts patient safety practices in the hospital.
We expect the implementation of this tool to radically change the workflow and speed of response of infection preventionists, greatly improving their ability to prevent HAI instead of reacting after they have occurred.
Study Type
Interventional
Enrollment (Estimated)
25
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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Ohio
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Columbus, Ohio, United States, 43210
- The Ohio State University
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Infection preventionist or physician involved in infection prevention at participating health system
Exclusion Criteria:
- Not an infection preventionist nor a physician involved in infection prevention
- Does not work at the participating health system
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: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: GeoHAI Use
Participants will use the GeoHAI tool
|
A Geographic healthcare-associated infection (HAI) visualization and assessment tool (GeoHAI) which uses spatio-temporal Bayesian models to identify clusters of National Healthcare Safety Network (NHSN)-defined hospital onset Clostridium difficile (CDI) and multidrug resistant organisms (MDRO), and predict potential high risk areas given hospital and patient risk factors.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline Healthcare-Associated Infection (HAI) Rate
Time Frame: Baseline and 3 months post-implementation
|
HAI rate at healthcare system level before intervention and after
|
Baseline and 3 months post-implementation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge of tool
Time Frame: Immediately post-training
|
Knowledge questions to assess understanding of how to use the GeoHAI tool, assessed after participants are trained on how to use the tool
|
Immediately post-training
|
|
Change from baseline skill confidence
Time Frame: Baseline, 1 month post-implementation
|
Self-reported level of confidence on investigating HAI clusters
|
Baseline, 1 month post-implementation
|
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Usability score
Time Frame: Immediately post training, 1 month post-implementation
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System Usability Scale score, and impacts of the tool on work and workflow (interruptions, workarounds, issues/challenges)
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Immediately post training, 1 month post-implementation
|
|
GeoHAI Use
Time Frame: 1 month post-implementation
|
Self-reported frequency of use of the GeoHAI tool
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1 month post-implementation
|
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Change in Healthcare-Associated Infection (HAI) Investigation Process
Time Frame: Baseline, 1 month post-implementation
|
Change in how infection preventionists investigate Healthcare-Associated Infections (HAIs)
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Baseline, 1 month post-implementation
|
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Number of months healthcare system is below goal HAI rate
Time Frame: Baseline, 3 months post-implementation
|
Monthly HAI rate at healthcare system level before intervention and after
|
Baseline, 3 months post-implementation
|
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Change in feasibility score
Time Frame: Immediately post training, 1 month post-implementation
|
Score on feasibility, acceptability, and appropriateness domains of validated Implementation Outcome scale (minimum score = 1, maximum score = 5, where higher scores indicate better feasibility)
|
Immediately post training, 1 month post-implementation
|
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Change in time to HAI cluster identification
Time Frame: Baseline, 3 months post-implementation
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Time from when an HAI test was ordered for the first positive patient ultimately contained in an identified HAI cluster, to when that HAI cluster is identified.
|
Baseline, 3 months post-implementation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Courtney Hebert, MD, Ohio State University
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 (Actual)
February 13, 2023
Primary Completion (Actual)
April 1, 2026
Study Completion (Estimated)
September 1, 2026
Study Registration Dates
First Submitted
April 18, 2022
First Submitted That Met QC Criteria
November 4, 2022
First Posted (Actual)
November 10, 2022
Study Record Updates
Last Update Posted (Actual)
May 5, 2026
Last Update Submitted That Met QC Criteria
April 29, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01HS027200 (U.S. AHRQ Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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