Improving Quality of Life After Thoracic Surgery Using Patient-Reported Outcomes

NACompletedINTERVENTIONAL
Enrollment

113

Participants

Timeline

Start Date

April 30, 2020

Primary Completion Date

November 10, 2023

Study Completion Date

November 10, 2023

Conditions
Thoracic Surgery
Interventions
OTHER

Active Monitoring

The participants randomized to active symptom monitoring will have alerts sent to their clinicians when their PRO symptom scores exceed baseline postoperative scores (when discharge day scores are available) by 2 points or more, or when 'severe' or 'very severe' symptoms are reported.

OTHER

Passive Monitoring

Participants randomized to the passive PRO monitoring arm will complete the same PROs as participants in the active monitoring arm, but will not have alerts sent to their clinician.

Trial Locations (1)

27599

University of North Carolina at Chapel Hill, Chapel Hill

All Listed Sponsors
collaborator

Thoracic Surgery Foundation

UNKNOWN

collaborator

American College of Surgeons

OTHER

lead

UNC Lineberger Comprehensive Cancer Center

OTHER

NCT04342260 - Improving Quality of Life After Thoracic Surgery Using Patient-Reported Outcomes | Biotech Hunter | Biotech Hunter