Improving Thoracic Surgical Care Using Electronic Patient-Reported Outcomes (ePROS)

Thoracic Clinical Trial

Official title: Improving Thoracic Surgical Care Using Electronic Patient-Reported Outcomes (ePROS)

Status Recruiting

Clinical Trial Summary

This is a single-site, non-randomized study on the outcomes of remote real-time "ePRO monitoring" in thoracic surgery patients. ePRO monitoring is a health information technology intervention comprised of delivering longitudinal electronic patient-reported outcome (ePRO) surveys (e.g., on symptoms, and physical functioning) coupled with automated provider alerts for concerning survey responses.

Clinical Trial Description

Thoracic surgery patients are at high risk for severe complications post-surgery, such as respiratory failure, empyema, wound problems, and even mortality. Patients with complications may need readmission and invasive management. Usual care may not capture the symptoms of surgery complications. Well-designed remote monitoring of postoperative patients may enable early intervention and lower the risk of severe complications.

This study evaluates the implementation and effectiveness of perioperative electronic patient-reported outcomes (ePROs) monitoring in thoracic surgery patients. Previous studies demonstrated the feasibility of ePROs monitoring by thoracic surgery patients and providers. This study will explore barriers to implementation before real-world effectiveness studies. ;

Related Conditions & MeSH terms

• Aortic Dissection
• Thoracic

• NCT number: NCT06075316
• Study type: Interventional
• Source: UNC Lineberger Comprehensive Cancer Center
• Contact: Amanda Gentry
• Phone: (336) 655-7743
• Email: Amanda_gentry@med.unc.edu
• Status: Recruiting
• Phase: N/A
• Start date: November 14, 2023
• Completion date: December 2026