Older Emergency Department Users and Short-term Adverse Events at the Index Visit
1 other identifier
observational
10,971
1 country
1
Brief Summary
This study evaluates the difference between PRISMA-7 and ER2 tool. There are some differences between PRISMA-7 and ER2 tool. The differences consist in evaluation criteria that are used to perform the both surveys. We suppose that evaluation criteria of PRISMA-7 is not accurately enough to calculate the length of hospital stay and to predict the short-term outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2019
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 11, 2019
CompletedFirst Posted
Study publicly available on registry
July 15, 2019
CompletedStudy Start
First participant enrolled
July 23, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2024
CompletedJuly 23, 2024
July 1, 2024
4.6 years
July 11, 2019
July 22, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Short-term adverse events
The adverse event is defined as an adverse outcome related to an ED encounter, this adverse event is related to ED care.
Around 10 months
Study Arms (1)
Observational
Each participant will be evaluated at Emergency Department based on ER2 screening tool (Emergency Room Evaluation and Recommendation Form). Six closed-ended format questions (i.e., yes versus no) composed ER2 assessment: 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 its type, and temporal disorientation (inability to give the current month and/or year).
Eligibility Criteria
In this study will be enrolled people who are 75 years and over, and who come at Emergency not only for medical reason but also for social.
You may qualify if:
- Being 75 years old and over
- Brought at Emergency on medical stretcher
You may not qualify if:
- Being less than 75 years old
- Never come at Emergency
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Jewish General Hospital
Montreal, Quebec, H3T 1E2, Canada
Study Officials
- PRINCIPAL INVESTIGATOR
Oliver Beauchet, MD
Jewish General Hospital
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD, Professor of Geriatrics
Study Record Dates
First Submitted
July 11, 2019
First Posted
July 15, 2019
Study Start
July 23, 2019
Primary Completion
March 1, 2024
Study Completion
July 1, 2024
Last Updated
July 23, 2024
Record last verified: 2024-07