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 @ 11:33 PM
Ignite Modification Date:
2025-12-25 @ 9:21 PM
NCT ID:
NCT02715856
Group ID:
EG001
Title:
Phase II (Mobile Surveillance)
Description:
Patients undergo standard face-to-face follow up visits as in Group I. Patients also undergo mobile surveillance comprising use of a mobile device application to send photos and videos to study staff and engage in video conferences at 3, 7, 13, and 25 weeks after surgery.
Monitoring Device: Undergo surgical wound and physical activity monitoring
Physical Activity Measurement: Undergo physical activity measurement
Quality-of-Life Assessment: Ancillary studies
Questionnaire Administration: Ancillary studies
Standard Follow-Up Care: Undergo standard follow-up care
Survey Administration: Ancillary studies
Deaths Number Affected:
5
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
52
Other Number Affected:
0
Other Number At Risk:
52
Study:
NCT02715856
Results Section:
NCT02715856
Adverse Events Module:
NCT02715856