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
Event Groups
| Title | Description | Deaths # Affected | Deaths # At Risk | Serious # Affected | Serious # At Risk | Other # Affected | Other # At Risk | View |
|---|---|---|---|---|---|---|---|---|
| Socio-evaluative Speech Stress Session | Participants attended two laboratory sessions order of these sessions was counterbalanced. At one of the sessions, they completed a 5-minute socio-evaluative speech task defending themselves against an alleged transgression (e.g., running a stop sign). Outcomes in this condition include responses to this stressor. | 0 | None | 0 | 63 | 0 | 63 | View |
| Control Session | Participants attended two laboratory sessions. Order of sessions was counterbalanced. Presented outcome data are for the control condition only. Participants rested quietly for the 5-minute task period. | 0 | None | 0 | 61 | 0 | 61 | View |