Skip to main content
Clinical Trials/NCT06350266
NCT06350266
Completed
N/A

Informing Low-acuity Emergency Department Patients of Non-emergent Healthcare Resources Following Discharge to Decrease Emergency Department Utilization

Geisinger Clinic1 site in 1 country6,242 target enrollmentApril 25, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Emergency Service, Hospital
Sponsor
Geisinger Clinic
Enrollment
6242
Locations
1
Primary Endpoint
Return to Geisinger ED
Status
Completed
Last Updated
last year

Overview

Brief Summary

The goal of this campaign is to reduce unnecessary visits to a Geisinger emergency department (ED)/encourage patients with high acuity visits to follow up with an appropriate Geisinger provider. In this campaign, patients will be assigned to receive or not receive outreach following ED discharge that is aligned with the goal. Outreach will occur via a text message, as well as information added to the patient's after visit summary, and will includecalls to action to see their Geisinger CMSL PCP either in person or virtually. The study will assess whether ED use differs across patients in different outreach conditions. It will also examine whether patients follow through on the message-specific calls to action in the messages differently across conditions.

Registry
clinicaltrials.gov
Start Date
April 25, 2024
End Date
December 27, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Amir Goren

Program Director, Behavioral Insights Team

Geisinger Clinic

Eligibility Criteria

Inclusion Criteria

  • \>= 18 years of age
  • Geisinger ED visit rated as low acuity (L4 or L5)
  • Discharged from Geisinger ED in past 24 hours

Exclusion Criteria

  • Cannot be contacted via the communication modality being used in the study (i.e., SMS), due to insufficient/missing contact information in the EHR or because the patient opted out
  • Admitted to hospital
  • Already included in intervention in past 365 days

Outcomes

Primary Outcomes

Return to Geisinger ED

Time Frame: within 120 days following day of discharge

ED visit (yes/no)

Study Sites (1)

Loading locations...

Similar Trials