- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01515488
Kiosk-Model Self-Triage System in the Pediatric Emergency Department
September 13, 2012 updated by: Valleywise Health
Assessing Utility of a "Kiosk Model" Self-Triage System in the Pediatric Emergency Department of A Tertiary Care Teaching Hospital
An audio-assisted self-triage kiosk in the Pediatric Emergency Department (ED) is expected to significantly reduce triage times, without any sacrifice of the quality of information that would be obtained by nurse-initiated triage.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
With the rapid evolution of consumer based information technology patients have the opportunity to become collaborative partners in their care.
In addition, by bridging information gaps and improving workflow efficiency, continuity of care is optimized and the potential risk for error is reduced.
Triage time for kiosk self-triage and nurse-initiated triage will be compared in terms of 1) triage time; 2) accuracy of medical history obtained; and 3) patient satisfaction.
Study Type
Interventional
Enrollment (Actual)
400
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
-
-
Arizona
-
Phoenix, Arizona, United States, 85008
- Maricopa Integrated Health System
-
-
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
No older than 16 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Between 0 and 18 years of age
- Registered in the Pediatric ED
- Accompanied by parent/guardian 18 years or older
- Version 3 Emergency Severity Index (ESI) of 3 to 5
- Parent or guardian able to communicate in English or Spanish
Exclusion Criteria:
- Deemed medically unstable
- ESI score of 1 or 2
- Incarcerated or in juvenile detention
- Parent/guardian unable to communicate in English or Spanish
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: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Self-triage kiosk
Audio-assisted self-triage kiosk for obtaining medical history and presenting problem(s)
|
Audio-assisted self-triage kiosk for obtaining medical history and presenting problem(s)
Other Names:
|
Experimental: Nurse-initiated triage
Nurse-initiated triage for obtaining medical history and presenting problem(s)
|
Nurse-assisted triage for obtaining medical history and presenting problem(s)
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Triage Time
Time Frame: From beginning of triage to completion of triage.
|
The time it takes for the patient to be triaged, compared across the kiosk and nurse-initiated triage conditions.
|
From beginning of triage to completion of triage.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Accuracy of Medical History
Time Frame: Upon completion of triage.
|
To check for accuracy of medical history information, two RAs approached enrolled parents during the course of their ED visit in the individual patient examination rooms.
The RAs conducted a brief face-to-face interview with parents and verified information from the nursing triage summary sheet (for non-kiosk users) and the printout of history sheet from the kiosk users, noting any discrepancies on a Discrepancy Rating Scale.
All historical discrepancies were categorized into three groups: major discrepancy, minor discrepancy and no discrepancy.
|
Upon completion of triage.
|
Patient Satisfaction
Time Frame: Upon completion of triage.
|
Custom survey with 4 items capturing satisfaction with Understanding, Ease of Answering Questions, Respect for Privacy, and Overall Feelings.
For each item, the lowest possible score was 1 and the highest possible score was 6.
For Understanding, the lowest actual score was 2 and the highest actual score was 6.
For Ease of Answering Questions, the lowest actual score was 2 and the highest actual score was 6.
For Respect for Privacy the lowest actual score was 3 and the highest actual score was 6.
For Overall Feelings, the lowest actual score was 3 and the highest actual score was 6.
For the (unweighted) average of all 4 items, the lowest possible score was 1 and the highest possible score was 6.
The lowest actual score was 3.5 and the highest actual score was 6.0.
|
Upon completion of triage.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Madhumita Sinha, MD, MHSM, Valleywise Health
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.
General Publications
- Morrison-Beedy D, Carey MP, Tu X. Accuracy of audio computer-assisted self-interviewing (ACASI) and self-administered questionnaires for the assessment of sexual behavior. AIDS Behav. 2006 Sep;10(5):541-52. doi: 10.1007/s10461-006-9081-y.
- Sinha M, Khor KN, Amresh A, Drachman D, Frechette A. The use of a kiosk-model bilingual self-triage system in the pediatric emergency department. Pediatr Emerg Care. 2014 Jan;30(1):63-8. doi: 10.1097/PEC.0000000000000037.
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
January 1, 2012
Primary Completion (Actual)
April 1, 2012
Study Completion (Actual)
April 1, 2012
Study Registration Dates
First Submitted
January 13, 2012
First Submitted That Met QC Criteria
January 23, 2012
First Posted (Estimate)
January 24, 2012
Study Record Updates
Last Update Posted (Estimate)
October 15, 2012
Last Update Submitted That Met QC Criteria
September 13, 2012
Last Verified
September 1, 2012
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2009-110
- R03HS020235-01A1 (U.S. AHRQ Grant/Contract)
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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