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:
2025-12-24 @ 9:15 PM
Ignite Modification Date:
2025-12-25 @ 7:04 PM
NCT ID:
NCT04652804
Group ID:
EG001
Title:
Arm 2: Medium Intensity Intervention (Minimal Risk)
Description:
4 weeks dispensation + support from patient navigator
Medium intensity HCV treatment adherence support: The medium intensity intervention will include standard of care dispensation of a 28-day supply of medication at entry, 4 weeks and 8 weeks. Participants will be assigned to a patient navigator (PN) and receive tailored patient navigation support for medication reminders, picking up medication refills (or home or field delivery of study medications), overcoming barriers as well as service linkage. Participant will be contacted by the PN at least once every two weeks.
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
5
Serious Number At Risk:
684
Other Number Affected:
1
Other Number At Risk:
684
Study:
NCT04652804
Results Section:
NCT04652804
Adverse Events Module:
NCT04652804