- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03163225
Opportunities in Outpatient Care
Characterizing and Quantifying Challenges and Opportunities in Outpatient Care
Study Overview
Status
Conditions
Detailed Description
The study will develop a first-pass taxonomy that classifies the causes and effects of challenges and opportunities of outpatient care leading to potentially avoidable ED and urgent care center visits.
The study will quantify the proportion of ED and urgent care center visits that result from a challenge or opportunity in outpatient care and classify the causes and outcomes according to the taxonomy. It will also define the 30 and 90 day episode costs of ED and urgent care center visits associated with a challenges and opportunities of outpatient care beginning the day of the ED or urgent care center visit.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Utah
-
Murray, Utah, United States, 84157
- Intermountain Medical Center
-
Murray, Utah, United States, 84107
- Cottonwood InstaCare
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Riverton, Utah, United States, 84065
- Riverton Hospital
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Riverton, Utah, United States, 84065
- Southridge InstaCare
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Salt Lake City, Utah, United States, 84143
- LDS Hospital
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Salt Lake City, Utah, United States, 84102
- Salt Lake City InstaCare
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Salt Lake City, Utah, United States, 84105
- Memorial InstaCare
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Sandy, Utah, United States, 84094
- Alta View Hospital
-
Sandy, Utah, United States, 84070
- Sandy InstaCare
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- All Emergency Department/IC patients who can consent, including children.
Exclusion Criteria:
- Unable to give consent
- Prisoners
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Incidence rate of avoidable ED visits due to a "missed" opportunity in outpatient care
Time Frame: 1 Day
|
The proportion of ED visits during the selected shifts that were deemed to be potentially avoidable according to the developed taxonomy
|
1 Day
|
|
Incidence rate of avoidable InstaCare visits due to a "missed" opportunity in outpatient care
Time Frame: 1 Day
|
The proportion of Instacare visits during the selected shifts that were deemed to be potentially avoidable according to the developed taxonomy
|
1 Day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient Disposition Status from the ED
Time Frame: 1 Day
|
Disposition status from after the ED visit, collected from the medical record.
Status will be one of the following: admitted, observation, transfer to facility, discharged, deceased.
|
1 Day
|
|
Patient Disposition Status from the InstaCare
Time Frame: 1 Day
|
Disposition status from after the Instacare visit, collected from the medical record.
Status may be admitted, observation, transfer to facility, discharged, or deceased.
|
1 Day
|
|
Length of stay for admitted patients
Time Frame: Up to 30 days
|
Length in stay by days in study patients admitted to the hospital
|
Up to 30 days
|
|
Harms to patients due to the missed opportunities in outpatient care.
Time Frame: 90 days
|
Categorization of the "harms" on patients due to the missed opportunities in outpatient care using NCC-MERP categorizations
|
90 days
|
|
30 day episode costs
Time Frame: 30 days
|
All attributable healthcare costs accrued to study patients from the date of visit to +30 days.
|
30 days
|
|
90 day episode costs
Time Frame: 90 days
|
All attributable healthcare costs accrued to study patients from the date of visit to +90 days.
|
90 days
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Todd Allen, MD, Intermountain Health Care, Inc.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 1050460
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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