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ED delirium & dementia screening & outpatient referral for Dementia (IMPACT Trial)
N/A
Waitlist Available
Led By Ula Hwang, MD
Research Sponsored by Yale University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights
IMPACT Trial Summary
This study is evaluating whether a process of screening, referral, and care coordination can improve outcomes for older ED patients who may have UCID.
Eligible Conditions
- Dementia
- Delirium
- Cognitive Impairment
- Emergency Care
IMPACT Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Number of Participants Diagnosed With Dementia Among Those With Completed Outpatient Assessment
Percentage of Patients With Confirmed Delirium or Dementia
Rates of Connection With Primary Care
+1 moreIMPACT Trial Design
1Treatment groups
Experimental Treatment
Group I: ED delirium & dementia screening & outpatient referralExperimental Treatment1 Intervention
Routine ED screening for delirium and memory problems with referral for outpatient assessment of cognitive impairment.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
PD4ED 3-step intervention (ED assessment, outpatient assessment, Brain health plan)
2021
N/A
~100
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Who is running the clinical trial?
Yale UniversityLead Sponsor
1,847 Previous Clinical Trials
2,736,428 Total Patients Enrolled
7 Trials studying Dementia
2,584 Patients Enrolled for Dementia
National Institute on Aging (NIA)NIH
1,668 Previous Clinical Trials
28,004,964 Total Patients Enrolled
265 Trials studying Dementia
23,623,311 Patients Enrolled for Dementia
Ula Hwang, MDPrincipal InvestigatorYale University
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