- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03471377
Improving Planned Surgical Case Duration Accuracy by Leveraging the EHR and Predictive Modeling
Improving Planned Surgical Case Duration Accuracy by Leveraging the EHR and Predictive Modeling - A Randomized Control Trial
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
New York
-
New York, New York, United States, 10065
- Memoral Sloan Kettering Basking Ridge
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- A surgeon or OR staff member in the Department of Surgery Gynecology and Colorectal service
Exclusion Criteria:
- Any new surgeon that starts their practice during the study
- Surgery will take place at a location other than the Main hospital or Josie Robertson Surgical Center
- Cases where input data was not available prior to the prediction generation including late add-on cases such as urgent and emergent cases that are placed on the schedule less than 24 hours before the surgery
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
standard scheduling process
Scheduling office assigns start time and room for case and places case on schedule.
At this point a default case duration is evaluated by the scheduling office, to see if the value is considered excessively short or excessively long.
|
Scheduling office assigns start time and room for case and places case on schedule.
At this point a default case duration is evaluated by the scheduling office, to see if the value is considered excessively short or excessively long.
Depending on the assessment, the scheduling office will either keep the default value, use the value that the surgeon placed in the notes (if available), or the scheduling office provides their own estimation.
|
|
assigned a planned case duration value from predictive model
Predictive model calculates new duration for case at 3AM the day before surgery, and the predictions are made available on a SecureShare-site.
|
Predictive model calculates new duration for case at 3AM the day before surgery, and the predictions are made available on a SecureShare-site. Model predictions are then read by scheduling manager sometime between 7am-10am from the SecureShare site, and the scheduling manager will in EPIC/OpTime, overwrite the current estimate with the new duration value that was generated by the predictive model. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
duration it takes surgeons to complete their respective surgical cases
Time Frame: 1 year
|
All Gynecology (GYN) and Colorectal (CRS) Surgeons at MSKCC will be included.
To test the hypothesis that the developed surgical case duration prediction model compared to the current process of estimating surgical case durations, will show improved prediction accuracy, measured by mean absolute error.
|
1 year
|
Collaborators and Investigators
Investigators
- Principal Investigator: Christopher Stromblad, Memorial Sloan Kettering Cancer Center
Publications and helpful links
Helpful Links
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
- 18-115
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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