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Coordinated Emergency Department Transitions

PartnerED Care: Coordinated Emergency Department Transitions for Assisted Living Patients With Alzheimer's Disease and Related Dementias

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06933849
Enrollment
1376
Registered
2025-04-18
Start date
2024-10-04
Completion date
2025-03-30
Last updated
2026-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer Disease or Associated Disorder

Keywords

case management, emergency department, feasibility

Brief summary

The goal of this observational study is to learn the feasibility, acceptability, appropriateness, and adherence to a case management intervention. PartnerED is a case management intervention that aims to reduce unnecessary hospital admissions by providing real-time, structured information and discharge support to emergency department providers via phone and fax. The intervention is led by chronic care managers employed by Bluestone Accountable Care Organization, a physician group primarily serving patients in assisted living centers.

Detailed description

PartnerED is a case management intervention that aims to reduce unnecessary hospital admissions by providing real-time, structured information and discharge support to emergency department providers via phone and fax. The intervention is led by chronic care managers employed by Bluestone Accountable Care Organization, a physician group primarily serving patients in assisted living centers.

Interventions

BEHAVIORALStructured case management

When a Bluestone Accountable Care Organization registers in an emergency department, a Bluestone chronic care manager contacts emergency department clinicians by phone and fax to provide up-to-date clinical and discharge support information.

Sponsors

Brown University
Lead SponsorOTHER
National Institute on Aging (NIA)
CollaboratorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Bluestone Accountable Care Organization patient * Registration in emergency department between November 1, 2023 and June 30, 2024, as recorded in electronic admission, discharge, and transfer notifications

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Percent of Eligible Emergency Department Visits With Completed OutreachWithin 1-3 hours of emergency department registrationPercent of eligible emergency department visits in which a case manager provided structured clinical and discharge support information to a emergency department provider about a patient who was in their care, with the goal of avoiding an unnecessary hospitalization

Secondary

MeasureTime frameDescription
Percent of Successful Outreach Conversations in Which Staff Reported Avoidance of an Unnecessary HospitalizationWithin 24 hours of emergency department registrationCase manager self-report of whether she/he was successful in avoiding an unnecessary hospitalization of a patient after providing structured clinical and discharge support information to the emergency department provider

Countries

United States

Contacts

PRINCIPAL_INVESTIGATOREllen McCreedy, PhD, MPH

Brown University

Baseline characteristics

Characteristic
Age, Continuous81.9 years
STANDARD_DEVIATION 12.4
Ethnicity (NIH/OMB)
Hispanic or Latino
19 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
1214 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
143 Participants
Race (NIH/OMB)
American Indian or Alaska Native
5 Participants
Race (NIH/OMB)
Asian
11 Participants
Race (NIH/OMB)
Black or African American
23 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
1 Participants
Race (NIH/OMB)
Unknown or Not Reported
126 Participants
Race (NIH/OMB)
White
1210 Participants
Region of Enrollment
United States
1376 Participants
Sex: Female, Male
Female
921 Participants
Sex: Female, Male
Male
455 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
3 / 1,376
other
Total, other adverse events
0 / 1,376
serious
Total, serious adverse events
0 / 1,376

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 28, 2026