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 @ 6:41 PM
Ignite Modification Date:
2025-12-25 @ 4:12 PM
NCT ID:
NCT03843957
Group ID:
EG006
Title:
Clinic Patients Eligible for CRC Screening on "High Touch" Strategy (Pre-Implementation)
Description:
English or Spanish-speaking patients aged 50-74 who are eligible for CRC screening who are seen in the study clinics randomized to mPATH utilizing the "high touch" implementation strategy but in 8 months before implementation.
"high touch" Implementation strategy: The "high touch" strategy consists of pre-implementation activities, training, and ongoing support.
Pre-Implementation Activities
* Clinic champion identified.
* Study team meeting with clinic champion
* Implementation adaptations as needed for clinic flow
Implementation Kick-Off (Day 1)
• On-site training with key clinic personnel
Months 1 - 6
* Phone/email technical support, as needed.
* Access to web-based QA dashboard
* Monthly program usage report sent to clinic champions
* Scheduled phone-calls with clinic champion to review QA data and explore potential barriers.
* Implementation adaptations as needed for clinic flow
* Goal-triggered follow-up on-site trainings
* Additional on-site trainings as requested.
Months 7 - 12
* Phone/email technical support, as needed
* Access to web-based QA dashboard
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
5526
Other Number Affected:
0
Other Number At Risk:
5526
Study:
NCT03843957
Results Section:
NCT03843957
Adverse Events Module:
NCT03843957