Adverse Events Module

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Adverse Events Module

For researchers submitting trial data to ClinicalTrials.gov, the Adverse Events module is one of four mandatory results sections. It requires reporting in three primary categories: All-Cause Mortality: A table tracking all deaths that occurred during the study, regardless of cause. Serious Adverse Events (SAEs): A tabular summary of events resulting in death, life-threatening conditions, hospitalization, or significant disability. Other Adverse Events: A table for non-serious events that exceed a specific frequency threshold, such as 5% within any study arm.

Adverse Events Module path is as follows:

Study -> Results Section -> Adverse Events Module -> Event Groups

Study -> Results Section -> Adverse Events Module -> Serious Events

Study -> Results Section -> Adverse Events Module -> Other Events

Adverse Events Module

Ignite Creation Date: 2025-12-24 @ 5:58 PM
Ignite Modification Date: 2025-12-25 @ 3:21 PM
NCT ID: NCT02370368
Description: At the beginning and end of every training session participants were asked to indicate if they had any aches, pains or injuries. They were asked to indicate all problems even if they did not think it was related to the training programme.
Frequency Threshold: 0
Time Frame: Data on adverse events was collected for the duration of the study which ran from September 2014 to January 2015. Persons were assessed at the beginning and end of every training session for the entire duration of the study's intervention, approximately six weeks per participant. Participants were advised that they could report any adverse events at any point during the research process.
Study: NCT02370368
Study Brief: Comparison of Videogame Based Dance Training With Agility Ladder Drills on Agility of Volleyball Players
Event Groups(If Any):

Event Groups

Title Description Deaths # Affected Deaths # At Risk Serious # Affected Serious # At Risk Other # Affected Other # At Risk View
Dance Training Participated in dance training with the XBOX Kinect 3 days per week for six weeks. 0 None 0 8 1 8 View
Ladder Drills Participated in a ladder drill training programme three times per week for six weeks. 0 None 0 7 2 7 View
Serious Events(If Any):
Other Events(If Any):

Other Events

Term Type Organ System Vocab View
Minor musculoskeletal strain SYSTEMATIC_ASSESSMENT Musculoskeletal and connective tissue disorders None View