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Informing Low-acuity Emergency Department Patients of Non-emergent Healthcare Resources Following Discharge to Decrease Emergency Department Utilization (2)
The goal of this campaign is to reduce unnecessary visits to a Geisinger emergency department (ED). In this campaign, patients will be assigned to receive or not receive outreach following ED discharge with a low-acuity visit designation. Outreach will occur via a text message the day after discharge from the ED as well as information added to the patient's after visit summary (AVS). Depending on the assigned condition, it will include calls to see their primary care provider (PCP) or use an Intelligent Triage tool. The study will assess whether ED use within the following 120 days differs across patients in different outreach conditions (current standard practice vs contact your PCP vs use Intelligent Triage). It will also examine whether patients follow through on the message-specific calls to action differently across conditions.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Geisinger
Danville, Pennsylvania, United States
Start Date
April 15, 2025
Primary Completion Date
May 1, 2026
Completion Date
August 1, 2026
Last Updated
March 13, 2026
8,286
ESTIMATED participants
Contact your PCP
BEHAVIORAL
Use Intelligent Triage
BEHAVIORAL
Lead Sponsor
Geisinger Clinic
NCT06359210
NCT06491290
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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