Adverse Events Module

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 @ 3:28 PM
Ignite Modification Date: 2025-12-25 @ 1:44 PM
NCT ID: NCT02667392
Description: The original study design was to have two arms: 1) Biofeedback arm, 2) Verbal feedback arm. Secondary to construction of the laboratory space where the study was to take place and delayed human resources hiring of study personnel, recruitment for this study was delayed. It was determined that the most prudent course of action to study the efficacy of this experimental biofeedback intervention would be to conduct a single-arm study with all participants being assigned to the biofeedback arm.
Frequency Threshold: 0
Time Frame: Each participant was enrolled in the study for six weeks. Adverse Event data was collected for the six weeks participants were enrolled in the study.
Study: NCT02667392
Study Brief: Biofeedback to Increase Propulsion During Walking After Stroke
Event Groups(If Any):

Event Groups

Title Description Deaths # Affected Deaths # At Risk Serious # Affected Serious # At Risk Other # Affected Other # At Risk View
Biofeedback Group Participants will wear a pressure-sensitive insole inside the shoe of their paretic limb. An auditory tone will sound when participants have provided sufficient load to active the pressure-sensitive in-sole. Gait Training with Biofeedback: Intervention (12, 60-minute sessions, 3 times/week for four weeks) will occur in an outpatient research setting. Participants will be supervised by a licensed physical therapist and wear a gait belt during all activities. The therapist will choose from a standardized bank of gait activities, suitable to each participant's ability level. The goal for total walking time for each session will be 50 minutes: 5, 10-minute bouts with a 2-minute rest between bouts. This is the typical length and intensity of outpatient rehabilitation sessions for ambulatory patients discharged from inpatient rehabilitation. Biofeedback Group: Biofeedback (external-focus feedback) will be provided as an adjuvant to therapist-provided feedback during the intervention. Participants will be instructed that a tone will sound when they "push off with their (paretic) leg to swing it forward" when the participant-specific pre-programmed threshold is exceeded. 0 None 0 11 0 11 View
Serious Events(If Any):
Other Events(If Any):