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Improving Thoracic Surgical Care Using Electronic Patient-Reported Outcomes (ePROS)
Recruiting
Who can join
Ages 18 to 99 · All sexes
Full eligibility criteria
Inclusion Criteria: Patients participating in ePRO monitoring must meet the following inclusion criteria to participate in this study: 1. 18 years or older 2. English or Spanish speaking 3. Able to complete a web-based, telephonic (IVR), or CRA (or other IRB-approved research team member)-administrated symptom survey 4. Planned to undergo major thoracic surgery (involving chest wall incisions and overnight admission) 5. Discharged from the thoracic surgery service 6. Discharged to home Exclusion Criteria: All patients meeting any of the following exclusion criteria at enrollment will be excluded from study participation: 1. Not completing planned surgery within 3 months of obtaining informed consent 2. Inability to understand English or Spanish 3. Having undergone only minor thoracic surgery (e.g. bronchoscopy, cervical mediastinoscopy) 4. Dementia, altered mental status, or any psychiatric condition determined by the thoracic surgery provider team that would prohibit the understanding or rendering of informed consent. 5. Current incarceration 6. Pregnancy
About the study
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.
What is being tested
- Symptom monitoring (other)
Sponsor: UNC Lineberger Comprehensive Cancer Center · Participants: 200 · Started: Nov 14, 2023
Contact the study team
- Amanda Gentry · Phone: (336) 655-7743
Official record on ClinicalTrials.gov — NCT06075316
Locations in the U.S.
| North Carolina | Lineberger Comprehensive Cancer Center at University of North Carolina, Chapel Hill, Chapel Hill |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.