IMPACT: Pathway to Detection & Differentiation of Delirium & Dementia in the Emergency Department

Sponsor
Yale University (Other)
Overall Status
Completed
CT.gov ID
NCT04846322
Collaborator
National Institute on Aging (NIA) (NIH)
100
2
1
14.5
50
3.5

Study Details

Study Description

Brief Summary

This is an observational study of the pragmatic implementation of an ED screening, outpatient referral, and care coordination process for older ED patients who may have UCID.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: PD4ED 3-step intervention (ED assessment, outpatient assessment, Brain health plan)
N/A

Detailed Description

Embedded pragmatic, implementation pilot that incorporates training, ED assessment for delirium and dementia risk, referral of ED patients with undiagnosed cognitive impairment and dementia for primary care feedback and care recommendations. This pilot would gather observational data evaluating the feasibility of incorporating cognitive impairment screens into routine ED delirium assessments, and developing optimal work flow for identifying and referring ED patients with suspected (undiagnosed) dementia for confirmatory evaluation and care coordination.

Study Design

Study Type:
Interventional
Actual Enrollment :
100 participants
Allocation:
N/A
Intervention Model:
Sequential Assignment
Masking:
None (Open Label)
Primary Purpose:
Screening
Official Title:
Pathway to Detection & Differentiation of Delirium & Dementia in the Emergency Department
Actual Study Start Date :
Apr 1, 2021
Actual Primary Completion Date :
Jun 15, 2022
Actual Study Completion Date :
Jun 15, 2022

Arms and Interventions

Arm Intervention/Treatment
Other: ED delirium & dementia screening & outpatient referral

Routine ED screening for delirium and memory problems with referral for outpatient assessment of cognitive impairment.

Diagnostic Test: PD4ED 3-step intervention (ED assessment, outpatient assessment, Brain health plan)
ED assessment for suspected dementia. positive ED patients referred for outpatient clinic cognitive impairment assessment. positive clinic patients referred to primary care with brain health patient plan.

Outcome Measures

Primary Outcome Measures

  1. ED screening rates of delirium vs. suspected dementia [30 days]

    Number of patients 75+ screened / total number of ED visit by patients 75+

  2. Detection rates of delirium vs. suspected dementia [30 days]

    daily number of patients discharged from ED with positive suspected dementia screen / number of patients 75+ screened.

  3. Rates of outpatient assessment referral of patients with suspected dementia [30 days]

    number of patients with appointment to ADC or geriatrics outpatient clinic / number of patients given information sheet or referred to outpatient clinic

  4. Rates of confirmed dementia or mild cognitive impairment [30 days]

    number of patients positive for dementia or MCI / number of patients from ED seen at clinic with completion of UDS assessment

  5. Rates of connection with primary care [30 days]

    number of patients with PCP follow-up about brain health plan / number of patients with outpatient confirmation of Dementia or MCI

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adults age 65 or older

  • Discharged from the adult ED at YNHH or the ED at NMH

Exclusion Criteria:
  • Documented or known history of dementia

  • Alcohol/substance intoxication while in the ED

  • Non-English or Non-Spanish speaking

Contacts and Locations

Locations

Site City State Country Postal Code
1 Yale New Haven Hospital New Haven Connecticut United States 06512
2 Northwestern Chicago Illinois United States 60611

Sponsors and Collaborators

  • Yale University
  • National Institute on Aging (NIA)

Investigators

  • Principal Investigator: Ula Hwang, MD, Yale University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Yale University
ClinicalTrials.gov Identifier:
NCT04846322
Other Study ID Numbers:
  • 2000029490
  • U54AG063546
First Posted:
Apr 15, 2021
Last Update Posted:
Aug 9, 2022
Last Verified:
Aug 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Yale University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 9, 2022