Event Group

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 @ 4:06 AM
Ignite Modification Date: 2025-12-26 @ 3:03 AM
NCT ID: NCT03925220
Group ID: EG002
Title: Nutrition, Physical Activity, and Weight Talk Comparison - Parents
Description: For the comparison condition, after the baseline assessment, parents received a handbook on nutrition and physical activity entitled: "Healthy Eating \& Physical Activity Across Your Lifespan: Helping your Child - Tips for Parents". This handbook, which is adapted from the handbook developed by the National Institute of Diabetes and Digestive and Kidney Diseases and the Weight Control Information Network, is approximately the same length as the intervention handbook and is available in English and Spanish. It is given with an insert on reducing weight talk and weight teasing in the family. Parents also received a magnet with a message about nutrition and exercise. To control for contact time, these participants met live with a study staff member two weeks after receiving the handbook, completed an action plan, and had the 30-minute call, as well as receive two text messages twice per week for 13 weeks with tips and reminders from the comparison handbook and insert. Improving nutrition and physical activity among youth: A brief intervention focused on improving nutrition and physical activity among youth
Deaths Number Affected: 0
Deaths Number At Risk: None
Serious Number Affected: 0
Serious Number At Risk: 201
Other Number Affected: 0
Other Number At Risk: 201
Study: NCT03925220
Results Section: NCT03925220
Adverse Events Module: NCT03925220