Improving Thoracic Surgical Care Using Electronic Patient-Reported Outcomes (ePROS)
Recruiting
N/A
Interventional Study
Thoracic
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 99
- Sex
- Any
- Study type
- Interventional
- Purpose
- Health Services Research
- Participants needed
- 200 (estimated)
- Sponsor
- UNC Lineberger Comprehensive Cancer Center · Other
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About This Trial
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.
Trial Locations
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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)-administ…
Contacts