CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 2,793 enrolled
Drug / intervention
Team Monitoring +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03178045
NCT03178045N/ACompleted

Ambulatory Cancer Care Electronic Symptom Self-Reporting for Surgical Patients

Memorial Sloan Kettering Cancer Center·observational·Posted Jun 6, 2017·Updated Jun 23, 2023

In Brief

An observational study evaluating Team Monitoring and Enhanced Feedback for Patient Reported Outcomes. Completed, enrolled 2,793 participants across 1 site.

Detailed Summary

The aim of this study is to understand and improve the experience of patients after surgery by comparing two methods of following symptoms while the patient recovers at home.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedJun 6, 2017
Enrollment StartMay 31, 2017
Primary CompletionOct 30, 2019
Study CompletionMay 25, 2023
TodayJul 2, 2026
Enrollment to primary: 2.4 yearsPosted 9.1 years ago

Interventions

Team Monitoringother

In this cohort, the electronic system will provide advanced informatics support for push notifications to the care team based on the severity of the symptoms reported. This platform promotes early detection and intervention. The care team is alerted when patients experience symptoms out of the expected range or if symptoms are worsening. Nurses receive secure message notifications and will contact the patient by phone depending on symptom severity. If a patient responds with a moderate-severe answer, the office team gets an alert and calls the patient during business hours.

Enhanced Feedbackother

In this cohort, the electronic system will provide tailored normative data visualizations that offer context and education to patients regarding expected symptom severity. The information provided to patients in the Enhanced Feedback group will be procedure specific and based on continuously updated PRO-CTCAE data from previous patients. Patients are thus able to see their own recovery trajectory relative to that of patients who have undergone the same procedure. Care is patient activated in that patients will use the information about expected symptoms to decide whether they should call the care team (e.g., if they are experiencing symptoms that are more severe or more prolonged than expected). If a patient reports severe symptoms, they are instructed to immediately contact their physician's office or seek medical attention.