Status:
COMPLETED
Pre-Implementation Study of Improving Thoracic Surgical Care Using Electronic Patient-Reported Outcomes (ePROS)
Lead Sponsor:
UNC Lineberger Comprehensive Cancer Center
Collaborating Sponsors:
National Heart, Lung, and Blood Institute (NHLBI)
Conditions:
Thoracic Surgery
Eligibility:
All Genders
18-99 years
Brief Summary
The purpose of the LCCC 2202 is to evaluate the barriers and facilitators to implementing perioperative "ePRO monitoring". This study will inform a future hybrid effectiveness study (LCCC 2141:Improvi...
Detailed Description
This is a single-site, non-randomized study in patients receiving major thoracic surgery, which commonly involves chest wall incisions and overnight admission Eligible patients will be approached at a...
Eligibility Criteria
Inclusion
- 18 years or older
- English speaking
- Able and willing to complete a web-based or telephonic symptom survey
- Planned to undergo surgery within 90 days or have undergone and been discharged from major thoracic surgery within the last 30 days.
Exclusion
- Not completing planned surgery within 3 months of obtaining informed consent (for subjects recruited preoperatively)
- Inability to read and speak English
- Planned for foregut surgery (e.g. paraesophageal hernia repair, esophageal resection or repair)
- Having undergone only minor thoracic surgery (e.g. bronchoscopy, cervical mediastinoscopy)
- Dementia, altered mental status, or any psychiatric condition as determined by thoracic surgery provider team that would prohibit the understanding or rendering of informed consent.
- Current incarceration
- Pregnancy
Key Trial Info
Start Date :
April 7 2022
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
October 10 2022
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT05311670
Start Date
April 7 2022
End Date
October 10 2022
Last Update
December 20 2023
Active Locations (1)
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1
University of North Carolina at Chapel Hill
Chapel Hill, North Carolina, United States, 27599