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Clinical Trial Summary

This study plans to learn more about specific breathing and activity recommendations for patients after surgery. Participants will be monitored after abdominal surgery to identify what activities help them breathe better and reduce complications after surgery.


Clinical Trial Description

Investigators will study adults undergoing elective abdominal surgery with at least moderate risk for postoperative pulmonary complications. Participants will be monitored on their chest and thigh with devices that record their breathing pattern (breath volume and frequency) and body position and movements. These monitors will be placed on their skin in the Post-Anesthesia Care Unit (PACU) and will stay on for three days, or until the patient is able to ambulate freely or until their hospital discharge, whichever comes earlier. Investigators will analyze the association between the frequency, duration and intensity of various activities (e.g., sitting, walking) and breathing and other clinical complications, in combination with medications received and other hospital course events. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06239831
Study type Observational
Source University of Colorado, Denver
Contact Emily G. Helmer
Phone (303)-724-2938
Email emily.helmer@cuanschutz.edu
Status Recruiting
Phase
Start date December 22, 2022
Completion date June 22, 2025

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