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

ConditionThoracic
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-99
SponsorUNC Lineberger Comprehensive Cancer Center

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.

Eligibility criteria

Qualifiers

18 years or older

English or Spanish speaking

Able to complete a web-based, telephonic (IVR), or CRA (or other IRB-approved research team member)-administrated symptom survey

Planned to undergo major thoracic surgery (involving chest wall incisions and overnight admission)

Disqualifiers

Not completing planned surgery within 3 months of obtaining informed consent

Inability to understand English or Spanish

Having undergone only minor thoracic surgery (e.g. bronchoscopy, cervical mediastinoscopy)

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.

Trial design

Treatments tested in this trial

  • Symptom monitoring

Treatment groups

200 Participants
are divided into 1 treatment group

Sponsors and collaborators

UNC Lineberger Comprehensive Cancer Center

Lead sponsor

National Heart, Lung, and Blood Institute (NHLBI)

Collaborator