Cognitive Impairment in Older Emergency Department Users and Associated Adverse Outcomes

Active, not recruitingOBSERVATIONAL
Enrollment

4,724

Participants

Timeline

Start Date

January 17, 2020

Primary Completion Date

February 1, 2022

Study Completion Date

February 1, 2025

Conditions
Cognitive FrailtyPhysical FrailtyOlder Emergency Department Users
Interventions
OTHER

Observational

"ER2 is a simple and standardized clinical tool. The results of the questionnaires performed in ER2 study will be used. The assessment component of ER2 consists of 6 very simple closed-ended format questions (i.e., yes versus no) which are: Age category (≥ 85), male, polypharmacy (≥ 5 different medications per day), use of formal (health care or social professional) and/or informal (family and/or friend) home support, use of a walking aid regardless of its type, and temporal disorientation (inability to give the current month and/or year). A score of five points is assigned to the items use of walking aid and temporal disorientation, whereas, for the other items, the assigned score is one point. The weighting of points for ER2 items is based on the results of our previous studies. Scores range from 0 (lowest risk) to 14 (highest risk). ER2 scores stratify the risk for short-term ED adverse events into three levels: low, moderate and high."

Trial Locations (1)

H3T 1E2

Jewish General Hospital, Montreal

All Listed Sponsors
lead

Jewish General Hospital

OTHER

NCT04235738 - Cognitive Impairment in Older Emergency Department Users and Associated Adverse Outcomes | Biotech Hunter | Biotech Hunter