Clinical Trials Directory

Trials / Completed

CompletedNCT05311670

Pre-Implementation Study of Improving Thoracic Surgical Care Using Electronic Patient-Reported Outcomes (ePROS)

Status
Completed
Phase
Study type
Observational
Enrollment
40 (actual)
Sponsor
UNC Lineberger Comprehensive Cancer Center · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

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:Improving Thoracic Surgical Care Using Electronic Patient-Reported Outcomes (ePROS). Eligible thoracic surgery patients will be enrolled to ePRO monitoring using web-based or telephone surveys. Patients will be asked to self-report symptoms for remote monitoring by their care team. Patients will be approached for a semi-structured interview to understand the barriers and facilitators to ePRO use.

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 any time point between their preoperative clinic visit and up to 30 days after discharge from the hospital. Approximately 60 patients will be enrolled in the study. Patients will complete symptom surveys via email or telephone. Concerning symptoms will generate alerts for the clinical care team who will follow their usual protocols for the management of symptoms. Patients will be purposively selected and invited to participate in a semi-structured interview to understand their experience using ePRO. Interviews will continue until 30 complete interviews are obtained and/or thematic saturation is reached.

Conditions

Interventions

TypeNameDescription
BEHAVIORALPatient-reported outcomes monitoringo Patient-reported outcomes will be collected from patients through web or telephone and alerts sent to providers.

Timeline

Start date
2022-04-07
Primary completion
2022-10-10
Completion
2022-10-10
First posted
2022-04-05
Last updated
2023-12-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05311670. Inclusion in this directory is not an endorsement.