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Clinical Trial Summary

This study will assess whether non-pharmacological interventions by a comfort coach affect the amount of opioid pain medication used, as well as perceived physical pain and emotional anxiety and healthcare utilization for adult cardiac surgery patients. Participants that are eligible for the study will be randomized to the comfort coach arm or standard of care. Both groups will complete surveys at the specific time frames in order to compare their outcomes. The study hypothesis is that there will be a decrease in opioid use in the intervention group compared to the standard of care arm during the 90-day perioperative course, as well as a decrease in pain and anxiety along with a lower composite outcome of healthcare utilization.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04051021
Study type Interventional
Source University of Michigan
Contact
Status Completed
Phase N/A
Start date September 4, 2019
Completion date January 5, 2021

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