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Efficiency And Quality In Post-Surgical Pain Therapy After Discharge — EQUIPPED  

Opioid Use Clinical Trial

Official title:
Efficiency And Quality In Post-Surgical Pain Therapy After Discharge

Clinical Trial Summary

Following inpatient surgery, more than 80% of patients are prescribed opioids for use after discharge, yet up to 90% of patients report leftover opioids, and only 16% maximize non-opioid therapy. The proposed research seeks to test a provider-facing decision support tool and a patient-facing smartphone app to reduce the amounts of opioids prescribed and taken following discharge, while ensuring effective treatment of pain after surgery.

Clinical Trial Description

Prior to discharge from the hospital, patients will be approached regarding interest in the study with an introductory letter that describes the content and purpose of the study. Following informed consent, patients will be randomized to receive the consumer health informatics app (UControlPain) versus provision of an app with only data collection function (no educational components). Randomization will be implemented via REDCap by the study coordinators. Further, information on which type of app was installed will not be shared with providers or patients. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05221866
Study type Interventional
Source University of Nebraska
Contact
Status Completed
Phase N/A
Start date March 14, 2022
Completion date December 10, 2023
View Details
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