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CMSL Ambulatory Sensitive Condition Nudge

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Geisinger Health

Status

Completed

Conditions

Emergency Department Visits
Nurse Care Coordination
Behavioral Intervention

Treatments

Behavioral: Nurse Nudge

Study type

Interventional

Funder types

Other

Identifiers

NCT06798389
2023-1716

Details and patient eligibility

About

The project aims to evaluate a nurse-led intervention to reduce inappropriate emergency department (ED) use among adult patients seen at Geisinger's Community Medicine Service Line (CMSL) clinics. The intervention occurs immediately following an appointment where they received a diagnosis of an ambulatory sensitive condition (ASC). The evaluation will compare eligible patients with an ASC who were randomly assigned to receive follow-up outreach from a nurse (who was automatically prompted via the Epic electronic health record system to initiate outreach) with those who were randomly assigned to receive standard care. Analyses will be intent-to-treat. The primary outcome is ED use in the week following the appointment.

Enrollment

3,016 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Age 18 years +
  • Has a visit in CMSL with an ambulatory sensitive condition (ASC) encounter diagnosis

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

3,016 participants in 2 patient groups

Nurse Nudge
Experimental group
Description:
Nurses in CMSL clinics will receive a notification to provide follow-up outreach to patients after the patient receives an ambulatory sensitive diagnosis.
Treatment:
Behavioral: Nurse Nudge
Control
No Intervention group
Description:
Nurses in CMSL clinics will receive standard follow-up notifications, which may mean no notifications, after a patient has received an ambulatory sensitive diagnosis.

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Amir Goren, PhD

Data sourced from clinicaltrials.gov

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