Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-25 @ 12:36 AM
Ignite Modification Date:
2025-12-25 @ 10:44 PM
NCT ID:
NCT03892967
Group ID:
EG001
Title:
EHR-facilitated Collaborative Care (Intervention)
Description:
Participants were administered ePROMs during EHR-facilitated collaborative care (ECC) periods. Automated responses, matched to symptom type and intensity, appeared following a patient's report of an actionable symptom, defined as \>=4/10 on a numeric rating scale (NRS). For any actionable symptom, respondents were asked if they wanted to receive symptom-specific self-management resources. For severe symptoms, \>=7/10, respondents were asked if they wanted to work remotely with a Symptom Care Manager (SCM) to develop an individualized symptom management plan.
Participants who responded to \>=2 ePROMs were included in the analytic cohort.
Deaths Number Affected:
3192
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
24874
Other Number Affected:
0
Other Number At Risk:
24874
Study:
NCT03892967
Results Section:
NCT03892967
Adverse Events Module:
NCT03892967